HCID 18433364, compound → HCID 9912141, compound

HRID 2305636Notes

Reaction equation

HRID 2305636 reaction equation
C[O:2][C:3](=[O:15])[CH2:4][CH2:5][CH2:6][O:7][C:8]1[CH:13]=[C:12]([NH2:14])[CH:11]=[CH:10][CH:9]=1.[NH:16]([C:23]1[S:24][C:25]2[CH:31]=[C:30]([CH2:32][C:33](O)=[O:34])[CH:29]=[CH:28][C:26]=2[N:27]=1)[C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1>>[NH:16]([C:23]1[S:24][C:25]2[CH:31]=[C:30]([CH2:32][C:33]([NH:14][C:12]3[CH:11]=[CH:10][CH:9]=[C:8]([O:7][CH2:6][CH2:5][CH2:4][C:3]([OH:2])=[O:15])[CH:13]=3)=[O:34])[CH:29]=[CH:28][C:26]=2[N:27]=1)[C:17]1[CH:18]=[CH:19][CH:20]=[CH:21][CH:22]=1

Participants

3

Reactant 2

HCID 18433364HCID 18433364, compoundHCID 18433369HCID 18433369, compound

Product 1

HCID 9912141HCID 9912141, compound

Procedure

Methyl4-(5-aminophenoxy)butyrate was made as described in example 7 above and coupled with 2-anilino-6-carboxymethylbenzothiazole according to the method described in example 7 to produce the methyl ester of 2-anilino-6-{3-[3-carboxypropoxy]anilino carbonyl methyl}benzothiazole

Sources & evidence

ORD record
ord-ea59797392a34564ba0776ffccc7a82a
Source dataset
uspto-grants-2002_08
Patent number
US06441012B1

Reaction notes

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