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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Water → (6-Chloro-5-methylpyridin-3-yl)methanamine hydrochloride

HRID 711238
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HRID 711238 반응식
[N:1]([CH2:4][C:5]1[CH:6]=[C:7]([CH3:12])[C:8]([Cl:11])=[N:9][CH:10]=1)=[N+]=[N-].C1C=CC(P(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1.O>C1COCC1>[ClH:11].[Cl:11][C:8]1[N:9]=[CH:10][C:5]([CH2:4][NH2:1])=[CH:6][C:7]=1[CH3:12]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 962WaterHCID 11776TriphenylphosphineHCID 866797195-(Azidomethyl)-2-chloro-3-methylpyridine

생성물 1

HCID 53395592(6-Chloro-5-methylpyridin-3-yl)methanamine hydrochloride

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

To the solution of 5-(azidomethyl)-2-chloro-3-methylpyridine 30-3 (2.0 g, 11 mmol) in THF (20 mL) was added PPh3 (3.17, 12 mmol) slowly. After 2 hours, H2O was added to the reaction mixture and the reaction was stirred for additional 15 hours, and the solvent was removed. The crude product was partitioned between ethyl acetate (50 mL) and 0.2 N HCl (50 mL). The aqueous phase was dried to give (6-chloro-5-methylpyridin-3-yl)methanamine HCl salt 30-4 as a white solid.

후처리

  1. customthe solvent was removed
  2. customThe crude product was partitioned between ethyl acetate (50 mL) and 0.2 N HCl (50 mL)
  3. customThe aqueous phase was dried

출처 및 근거

ORD 기록
ord-ef5dfc70a84f455cb88af2762191b626
출처 데이터셋
uspto-grants-2015_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09181235B2

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