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Hydrochloric Acid → HCID 178478602, 화합물

HRID 325513
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HRID 325513 반응식
[NH2:1][C:2]1[C:6]([NH:7][CH2:8][CH2:9][CH2:10][O:11][C:12]2[CH:17]=[C:16]([CH2:18][N:19]3[CH2:24][CH2:23][CH2:22][CH2:21][CH2:20]3)[CH:15]=[CH:14][N:13]=2)=[N:5]S(=O)[N:3]=1.[ClH:26]>CO>[ClH:26].[ClH:26].[ClH:26].[N:19]1([CH2:18][C:16]2[CH:15]=[CH:14][N:13]=[C:12]([O:11][CH2:10][CH2:9][CH2:8][NH:7][C:6](=[NH:5])[C:2](=[NH:1])[NH2:3])[CH:17]=2)[CH2:24][CH2:23][CH2:22][CH2:21][CH2:20]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 313Hydrochloric AcidHCID 159613413-Amino-4-[3-(4-piperidinomethyl-2-pyridyloxy)propylamino]-1,2,5-thiadiazole 1-oxide

생성물 1

HCID 178478602HCID 178478602, 화합물

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

The product of Step B (5.0 g; 13.7 mmoles) was dissolved in 80 ml of methanol and treated with 9.1 ml of concentrated HCl. After stirring at ambient temperature for 4.5 hours, the solution was evaporated to dryness under reduced pressure to give the title compound.

후처리

  1. customthe solution was evaporated to dryness under reduced pressure
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출처 및 근거

ORD 기록
ord-4152373b8f634b8198566fb409dc9b3e
출처 데이터셋
uspto-grants-1984_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04440933

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