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Potassium hydroxy sulfite → 2-Chloro-4-morpholinopyrido[3,2-d]pyrimidine-6-carboxylic acid

HRID 1043582
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인쇄 미리보기

반응식

HRID 1043582 반응식
[Cl:1][C:2]1[N:3]=[C:4]([N:14]2[CH2:19][CH2:18][O:17][CH2:16][CH2:15]2)[C:5]2[N:11]=[C:10]([CH:12]=[O:13])[CH:9]=[CH:8][C:6]=2[N:7]=1.[OH:20]OS([O-])=O.[K+]>CN(C=O)C>[Cl:1][C:2]1[N:3]=[C:4]([N:14]2[CH2:15][CH2:16][O:17][CH2:18][CH2:19]2)[C:5]2[N:11]=[C:10]([C:12]([OH:20])=[O:13])[CH:9]=[CH:8][C:6]=2[N:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 23707502Potassium hydroxy sulfiteHCID 534880072-Chloro-4-morpholinopyrido[3,2-d]pyrimidine-6-carbaldehyde

생성물 1

HCID 584050092-Chloro-4-morpholinopyrido[3,2-d]pyrimidine-6-carboxylic acid

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

2-Chloro-4-morpholinopyrido[3,2-d]pyrimidine-6-carbaldehyde (0.56 g) was reacted with Oxone (1.1 eq) in DMF (10 mL) overnight. The DMF was removed under vacuum and the reaction mixture was brought up into water. The pH was adjusted to 2-3 and product crashed out of solution. The solid was collected by filtration and dried to afford 0.45 g of 2-chloro-4-morpholinopyrido[3,2-d]pyrimidine-6-carboxylic acid as a light yellow solid.

후처리

  1. customThe DMF was removed under vacuum
  2. filtrationThe solid was collected by filtration
  3. customdried

출처 및 근거

ORD 기록
ord-09fabb76c42f47fcac2a6b01a9ff9fa2
출처 데이터셋
uspto-grants-2013_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08563540B2

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